27 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 22, 2024
LOGIC TIBIA IMPLANT PSC INSERT, SZ 5, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 13, 2023
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 17, 2024
LOGIC FEMORAL PS CEM LEFT SZ 3.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 5, 2025
LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·June 30, 2022
LOGIC TIBIA IMPLANT PSC INSERT, SZ 3.5, 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 5, 2024
LOGIC TIBIA IMPLANT PSC INSERT, SZ 1, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 11, 2024
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 22, 2024
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 26, 2023
OPTETRAK LOGIC
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 7, 2023
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 11, 2023
INSERT TIBIA LOGIC PSC SZ3 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 7, 2020
LOGIC TIBIA IMPLANT PSC INSERT, SZ 3, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 30, 2024
LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 11, 2023
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·November 8, 2024
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·June 26, 2023
LOGIC TIBIA IMPLANT PSC INSERT, SZ 1, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 27, 2025
LOGIC TIBIA IMPLANT PSC INSERT, SZ 2, 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 1, 2022
LOGIC FEMORAL PS CEM RIGHT SZ 6
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·August 9, 2024
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·May 30, 2024